Systematic genome-wide mapping of host determinants of bacteriophage infectivity.

IF 7.7
Cell systems Pub Date : 2025-11-19 Epub Date: 2025-10-15 DOI:10.1016/j.cels.2025.101427
Chutikarn Chitboonthavisuk, Cody Martin, Phil Huss, Jason M Peters, Karthik Anantharaman, Srivatsan Raman
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Abstract

Bacterial host factors regulate the infection cycle of bacteriophages. Except for some well-studied host factors (e.g., receptors or restriction-modification systems), the contribution of the rest of the host genome on phage infection remains poorly understood. We developed phage-host analysis using genome-wide CRISPR interference and phage packaging ("PHAGEPACK"), a pooled assay that systematically and comprehensively measures each host gene's impact on phage fitness. PHAGEPACK combines CRISPR interference with phage packaging to link host perturbation to phage fitness during active infection. Using PHAGEPACK, we constructed a genome-wide map of genes impacting T7 phage fitness in permissive E. coli, revealing pathways that affect phage packaging. When applied to the non-permissive E. coli O121, PHAGEPACK identified pathways leading to host resistance; their removal increased phage susceptibility up to a billion-fold. Bioinformatic analysis indicates that phage genomes carry homologs or truncations of key host factors, potentially for fitness advantage. In summary, PHAGEPACK offers insights into phage-host interactions, phage evolution, and bacterial resistance.

噬菌体感染性宿主决定因素的系统全基因组图谱。
细菌宿主因子调控噬菌体的感染周期。除了一些被充分研究的宿主因子(如受体或限制性修饰系统)外,宿主基因组的其余部分对噬菌体感染的贡献仍然知之甚少。我们使用全基因组CRISPR干扰和噬菌体包装(“PHAGEPACK”)开发了噬菌体-宿主分析,这是一种系统和全面测量每个宿主基因对噬菌体适应性影响的汇集试验。PHAGEPACK将CRISPR干扰与噬菌体包装结合起来,将宿主摄动与活性感染期间的噬菌体适应性联系起来。利用PHAGEPACK,我们构建了一个影响T7噬菌体适应性的基因全基因组图谱,揭示了影响噬菌体包装的途径。当应用于非容性大肠杆菌O121时,PHAGEPACK确定了导致宿主耐药的途径;它们的去除将噬菌体的易感性提高了十亿倍。生物信息学分析表明,噬菌体基因组携带关键宿主因子的同源物或截断物,可能具有适应性优势。总之,PHAGEPACK提供了噬菌体-宿主相互作用,噬菌体进化和细菌耐药性的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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